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Recruiting

NCT Number: NCT07574905

Evaluation of Satisfaction and Experiences in Patients Undergoing Awake Intubation.

The aim of this observational study is to evaluate postoperative satisfaction and experiences in patients undergoing awake intubation.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Be eligible for awake intubation
  • Agree to participate in the study
  • Be aged 18 or over

Exclusion criteria

  • Having communication difficulties.
  • Patients requiring emergency surgery.
  • Refusing to take part in the study.

Treatment and study plan

awake intubation

Other

To evaluate the experiences and satisfaction of patients who underwent awake intubation.

Primary outcomes

  1. An assessment of patient satisfaction and experiences with the procedure in patients undergoing awake intubation using a questionnaire.

    Time frame: 24 hours postoperatively

    Participants rate the questions on a scale from 1 to 5. A score of 1 is interpreted as 'very poor', and a score of 5 as 'very good'.

Study contacts

Contact information is provided by the study sponsor or research team.

Aysun Ankay Yılbas

CONTACT

Ozge Ozen

CONTACT

[email protected]

+905396674959

Sponsors and collaborators

Lead sponsor

Hacettepe University

Other

Registry information

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
May 8, 2026
Registry last updated
May 8, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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